| ¿µ¹® | acoustic neuroma, acoustic neurilemmoma | ÇÑ±Û | û½Å°æÃÊÁ¾ |
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| ¼³¸í | û½Å°æ(Á¦8³ú½Å°æ)ÀÇ ½Å°æ°ÑÀ» ½Î°í ÀÖ´Â Áý(sheath)ÀÇ ½´¹Ý¼¼Æ÷(Schwann cell)¿¡¼ ±â¿øÇÏ´Â Á¾¾ç-³úÁ¾¾ç Áß ºñ±³Àû ÈçÇÏ¸ç ´ë°³ 40~50´ë¿¡ È£¹ßÇÑ´Ù. Áõ»óÀ¸·Î´Â ±Í¿ï¸², ³Ã», ¼Ò³ú±â´ÉÀå¾Ö µîÀÌ ÀÖÀ¸¸ç, ÀÌÁß ±Í¿ï¸²ÀÌ °¡Àå ÃʱâÀÇ Áõ»óÀÌ´Ù. |
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| ¿µ¹® | neurofibromatosis | ÇÑ±Û | ½Å°æ¼¶À¯Á¾Áõ |
|---|---|---|---|
| ¼³¸í | Àü½ÅÀÇ ¿©·¯°÷¿¡ ¹«´õ±â·Î ³ª´Â ½Å°æ¼¶À¯Á¾À» Ư¡À¸·Î ÇÏ´Â À¯Àü¼º Àü½Å º´. ¸»ÃÊ ½Å°æ»Ó ¾Æ´Ï¶ó ÁßÃß ½Å°æ°èµµ ħ¹üÇÒ ¼ö ÀÖ´Ù. ½Å°æ¼¶À¯Á¾Àº ÁÖ·Î Àü½ÅÀÇ ÇǺο¡ ¹ß»ýµÇÁö¸¸ ½Å°æ¾ó±â ȤÀº ³»Àå¿¡ »ý±â´Â ¼öµµ ÀÖ´Ù. ÇǺο¡´Â ¶ÇÇÑ °÷°÷¿¡ ƯÀ¯ÀÇ °¥»ö»ö¼Ò¹ÝÀ» º¸°Ô µÈ´Ù. °ñ°ÝÀÇ º¯ÇüÀ» ÀÏÀ¸Å³ ¼öµµ ÀÖ´Ù. ½Å°æÃÊÁ¾À̳ª ¾Ç¼º½Å°æÃÊÁ¾, ´õ¿íÀÌ ½Å°æ±³Á¾À̳ª ¼ö¸·Á¾ µîÀÇ µÎ°³³»Á¾¾çÀ» ÇÕº´ÇÔµµ ¾Ë·ÁÁ® ÀÖ´Ù. 1Çü(von Recklinghausen º´, ÀüÇüÀû ½Å°æ¼¶À¯Á¾Áõ)°ú 2Çü(ÁßÃßÇü ¶Ç´Â û°¢½Å°æ¼¶À¯Á¾Áõ)À¸·Î ±¸ºÐÇÑ´Ù. ÀüÇüÀû ½Å°æ¼¶À¯Á¾Áõ(1Çü)ÀÌ °¡Àå ¸¹ÀÌ ¹ß»ýÇÏ¸ç ´ÙÀ½°ú °°Àº 3°¡Áö ¼Ò°ßÀ» º¸Àδô. Áï ¨ç üǥ¸é, ü³» ¿©·¯ °÷¿¡ »êÀçµÇ¾î ¹ß»ýÇÏ´Â ¾ó±â¸ð¾ç½Å°æÁ¾, ¨è ¿ìÀ¯Ä¿ÇǹÝÁ¡, ¨é ¸®½¬(Lisch) °áÀý·Î ºÒ¸®´Â ȫäÀÇ Âø»ö°ú¿ÀÁ¾ÀÌ´Ù. 2ÇüÀº 1Çüº¸´Ù ¹ß»ýºóµµ°¡ Àû°í, Ư¡ÀûÀ¸·Î ¾çÂʼº û°¢½Å°æÁ¾ÀÌ ÀÖÀ¸¸ç, ¿ìÀ¯¹ÝÁ¡Àº º¸À̳ª ¸®½¬°áÀýÀº ¾ø´Ù. |
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| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
|---|---|
| NF | nafcillin; National Formulary; nephritic factor; neurofibromatosis; neurofilament; neutral fraction;... |
| NF1 | neurofibromatosis type I; nuclear factor 1 |
| NF2 | neurofibromatosis type II |
| NFNS | neurofibromatosis-Noonan syndrome |
| NF1 | NEUROFIBROMATOSIS TYPE 1 |
|---|---|
| NF | Neurofibromatosis |
| NF 1 | Neurofibromatosis |
| NF 1 | Neurofibromatosis 1 |
| NF 2 | Neurofibromatosis 2 |
| abortive neurofibromatosis | incomplete neurofibromatosis |
|---|---|
| genes, neurofibromatosis 1 | Tumour suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause neurofibromatosis 1. (12 Dec 1998) |
| genes, neurofibromatosis 2 | Tumour suppressor genes located on the long arm of human chromosome 22. Mutation or loss of these genes causes neurofibromatosis 2. (12 Dec 1998) |
| central type neurofibromatosis | Type I neurofibromatosis. Incomplete neurofibromatosis, multiple neurofibromas with minimal manifestations, perhaps limited to cafe-au-lait spots; individuals with minimal lesions may have offspring with severe involvement. Synonym: abortive neurofibromatosis. (05 Mar 2000) |
| neurofibromatosis | <oncology> One of the most common disorders in genetics, neurofibromatosis encompasses at least two diseases, designated NF-1 and NF-2. NF-1 or classic neurofibromatosis, is characterised by the familiar cafe- au-lait spots, axillary freckling, cutaneous and visceral neurofibromas (which sometimes undergo malignant transformation), gliomas, scoliosis, and Lisch nodules of the iris. NF-1 is associated with the the von Recklinghausen Neurofibromatosis locus that encodes the NF-1 protein, a GTPase activating protein which interacts with the ras proteins. The gene is located on chromosome 17. NF-2, also called acoustic or central neurofibromatosis, features neurofibromas restricted to the acoustic nerve (usually bilateral) and the central nervous system, skin lesions may or may not be present. The gene is located on chromosome 22. There are no biochemical markers of the disorder, but the cloning of both the NF-1 and NF-2 genes makes DNA-based diagnosis possible in some families. Both genes appear to be tumour suppressor genes. Both conditions are autosomal dominant, but the variable penetrance and expressivity and high frequency of new mutations make genetic counseling difficult. Inheritance: autosomal dominant. (29 Dec 1997) |
| neurofibromatosis 1 | A congenital autosomal dominant disorder characterised by developmental changes in the nervous system, muscles, bones, and skin especially in those derived from the embryonic neural crest. There are multiple cutaneous tumours and tumours of the peripheral and central nervous system. The disease has been linked to mutations of the nf1 gene on chromosome 17. (12 Dec 1998) |
| neurofibromatosis 2 | Severe autosomal dominant disorder characterised especially by bilateral acoustic neuromas as well as other multiple tumours including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the nf2 gene on chromosome 22. (12 Dec 1998) |
| acoustic | Pertaining to the sense of hearing, the organs of hearing, or the science of sounds; auditory. Acoustic duct, the auditory duct, or external passage of the ear. Acoustic telegraph, a telegraph making audible signals; a telephone. Acoustic vessels, brazen tubes or vessels, shaped like a bell, used in ancient theaters to propel the voices of the actors, so as to render them audible to a great distance. Origin: F. Acoustique, Gr. Relating to hearing, fr. To hear. A medicine or agent to assist hearing. Source: Websters Dictionary (01 Mar 1998) |
| acoustic agraphia | The inability to write from dictation. (05 Mar 2000) |
| acoustic aphasia | An impairment in comprehension of the auditory forms of language and communication, including the ability to write from dictation in the presence of normal hearing. Spontaneous speech, reading, and writing are not affected. Synonym: acoustic aphasia, word deafness. (05 Mar 2000) |
| acoustic area | The floor of the lateral recess of the fourth ventricle, extending medially to the limiting sulcus and overlying the cochlear and vestibular nuclei of the rhombencephalon. Synonym: area acustica. (05 Mar 2000) |
| acoustic cell | A hair cell of the organ of Corti. (05 Mar 2000) |
| acoustic crest | An elevation on the inner surface of the ampulla of each saemicircular duct; filaments of the vestibular nerve pass through the crista to reach hair cells on its surface; the hair cells are capped by the cupula, a gelatinous protein-polysaccharide mass. Synonym: crista ampullaris, acoustic crest, transverse septum. (05 Mar 2000) |
| acoustic enhancement | A manifestation of increased acoustic signal amplitude returning from regions beyond an object which causes little or no attenuation of the sound beam. Compare: acoustic shadow. (05 Mar 2000) |
| acoustic impedance | The resistance that a material offers to the passage of a sound wave (colloquial); a property of a medium computed as the product of density and sound propagation speed (characteristic acoustic impedance). Discontinuities in acoustic impedance are responsible for the echoes on which ultrasound imaging is based. Unit: the rayl. (05 Mar 2000) |
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